This trial is conducted in Europe. The aim of this trial is to investigate the pharmacodynamic properties (the effect of the investigated drug on the body) of NN1218 in subjects with type 1 diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
52
A single dose of 0.2 U/kg body weight for subcutaneous (s.c., under the skin) administration.
A single dose of 0.2 U/kg body weight for subcutaneous (s.c., under the skin) administration.
Novo Nordisk Investigational Site
Neuss, Germany
Area under the glucose infusion rate curve
Time frame: From 0 to 2 hours
Area under the glucose infusion rate curve
Time frame: From 0 to 12 hours
Maximum glucose infusion rate
Time frame: Within 0 to 12 hours after dosing
Time to maximum glucose infusion rate
Time frame: Within 0 to 12 hours after dosing
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